Asymmetric synthesis of monocyclic β-lactams: application of imines derived from chiral N-protected α-amino aldehydes in the staudinger reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference17 articles.
1. Palomo, C.; Cossío, F.P.; Ontoria, J.M.; Odriozola, J.M.; preceding paper.
2. Optically active N-protected .alpha.-amino aldehydes in organic synthesis
3. SYNTHESIS OF α-AMINOALDEHYDES AND α-AMINOKETONES. A REVIEW
4. Chiral control of the Staudinger reaction
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1. Microwave-Induced Enantiospecific Synthesis of trans-(3R,4R)-3-Acetoxy-4-aryl-1-(chrysen-6-yl)azetidin-2-ones via the Staudinger Cycloaddition Reaction of (+)-Car-3-ene with Polyaromatic Imines;Russian Journal of Organic Chemistry;2020-05
2. Asymmetric Synthesis of β-Lactams by the Staudinger Reaction;Organic Reactions;2018-04-04
3. Synthesis of ?-lactams with ? electron-withdrawing substituents;Tetrahedron;2012-12
4. An Efficient Synthesis of Optically Active trans-(3R,4R)-3-Acetoxy-4-aryl-1-(chrysen-6-yl)azetidin-2-ones Using (+)-Car-3-ene as a Chiral Auxiliary;Helvetica Chimica Acta;2011-12
5. Synthetic Aspects of Homochiral β-Lactams Derived from N-Protected α-Aminoimines Via Asymmetric [2+2] Cycloaddition Reaction;Bulletin des Sociétés Chimiques Belges;2010-09-01
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